Experimental Infection of Captive Red Foxes (Vulpes vulpes) with Mycobacterium bovis

In Europe, animal tuberculosis (TB) due to Mycobacterium bovis involves multi-host communities that include cattle and wildlife species, such as wild boar (Sus scrofa), badgers (Meles meles) and red deer (Cervus elaphus). Red fox (Vulpes vulpes) infections have also been recently reported in some TB endemic regions in the Iberian Peninsula and France, with some of the infected animals shedding M. bovis in urine and feces. In order to understand the pathogenesis of M. bovis infection in foxes and the associated risk of transmission, 12 captive foxes (6 females and 6 males) were inoculated orally with 2 × 107 colony-forming units of a French field isolate of M. bovis. Clinical samples (urine, feces and oropharyngeal swabs) were collected every four weeks and tested for molecular diagnosis and bacteriology. Serological responses were measured by IDEXX M. bovis Ab Test and Multi Antigen Print Immunoassay (MAPIA). At a post-mortem examination performed 12 weeks post infection (wpi), tissues were tested for the presence of M. bovis and associated gross and microscopic TB-like lesions. M. bovis was detected by PCR in bladder swabs of 3 animals at 12 wpi. It was also detected pre-mortem at different time points of the experiment in the oropharyngeal mucus of three individuals and in the feces of nine foxes, with two of them confirmed by bacteriology. All 12 foxes had at least 4 PCR positive samples (out of the 23 tested), and all but 1 fox had at least 1 culture positive sample. The culture negative fox was PCR positive in both retropharyngeal and mesenteric lymph nodes, in line with the results of the other animals. Seroconversion was observed in all foxes except one during the experiment, and in nine at the final time point. No gross visible lesions were found in any animal at the post-mortem examination. The histology showed small granulomas within the lymph nodes, tonsils, liver and lungs from eight animals, with the presence of few acid-fast bacilli. These results confirmed that all orally-infected foxes developed mild TB lesions but they were able to shed mycobacteria in about 75% of cases, 1 month post-infection (9 out 12 foxes). These results show that it is possible to induce typical TB infection experimentally in captive foxes, with measurable M. bovis excretion; such an experimental system could be useful for future evaluations of diagnostics and vaccines in this species.

[1]  M. Boschiroli,et al.  Mycobacterium bovis Infection in Red Foxes in Four Animal Tuberculosis Endemic Areas in France , 2020, Microorganisms.

[2]  P. Alves,et al.  Quantification of the Animal Tuberculosis Multi-Host Community Offers Insights for Control , 2020, Pathogens.

[3]  E. Gormley,et al.  Evaluation of the Dual Path Platform (DPP) VetTB assay for the detection of Mycobacterium bovis infection in badgers. , 2020, Preventive veterinary medicine.

[4]  S. Lesellier,et al.  Protective Effect of Oral BCG and Inactivated Mycobacterium bovis Vaccines in European Badgers (Meles meles) Experimentally Infected With M. bovis , 2020, Frontiers in Veterinary Science.

[5]  S. Lesellier,et al.  Detection of live M. bovis BCG in tissues and IFN-γ responses in European badgers (Meles meles) vaccinated by oropharyngeal instillation or directly in the ileum , 2019, BMC Veterinary Research.

[6]  P. Hendrikx,et al.  Infection of Wildlife by Mycobacterium bovis in France Assessment Through a National Surveillance System, Sylvatub , 2018, Front. Vet. Sci..

[7]  M. Boschiroli,et al.  Mycobacterium bovis Infection of Red Fox, France , 2018, Emerging infectious diseases.

[8]  R. Juste,et al.  Immunohistochemical characterization of tuberculous lesions in sheep naturally infected with Mycobacterium bovis , 2018, BMC Veterinary Research.

[9]  S. Lesellier,et al.  Assessment of the safety of Bacillus Calmette-Guérin vaccine administered orally to badgers (Meles meles). , 2018, Vaccine.

[10]  H. Vordermeier,et al.  Differential Cell Composition and Cytokine Expression Within Lymph Node Granulomas from BCG‐Vaccinated and Non‐vaccinated Cattle Experimentally Infected with Mycobacterium bovis , 2017, Transboundary and emerging diseases.

[11]  S. Lesellier,et al.  The Effect of Oral Vaccination with Mycobacterium bovis BCG on the Development of Tuberculosis in Captive European Badgers (Meles meles) , 2017, Front. Cell. Infect. Microbiol..

[12]  R. Delahay,et al.  Sheep as a Potential Source of Bovine TB: Epidemiology, Pathology and Evaluation of Diagnostic Techniques. , 2016, Transboundary and emerging diseases.

[13]  A. Coelho,et al.  New Insights into Mycobacterium bovis Prevalence in Wild Mammals in Portugal. , 2016, Transboundary and emerging diseases.

[14]  E. Travis,et al.  The variability and seasonality of the environmental reservoir of Mycobacterium bovis shed by wild European badgers , 2015, Scientific Reports.

[15]  M. Palmer,et al.  Rapid Detection of Serum Antibody by Dual-Path Platform VetTB Assay in White-Tailed Deer Infected with Mycobacterium bovis , 2013, Clinical and Vaccine Immunology.

[16]  N. Smith,et al.  Comparative pathology of the natural infections by Mycobacterium bovis and by Mycobacterium caprae in wild boar (Sus scrofa). , 2013, Transboundary and emerging diseases.

[17]  N. Smith,et al.  Histological and immunohistochemical characterisation of Mycobacterium bovis induced granulomas in naturally infected fallow deer (Dama dama). , 2012, Veterinary immunology and immunopathology.

[18]  Graham C. Smith,et al.  Bacillus Calmette-Guérin vaccination reduces the severity and progression of tuberculosis in badgers , 2011, Proceedings of the Royal Society B: Biological Sciences.

[19]  Mahavir Singh,et al.  Oral vaccination of badgers (Meles meles) with BCG and protective immunity against endobronchial challenge with Mycobacterium bovis. , 2010, Vaccine.

[20]  M. Chambers,et al.  A review of infection of wildlife hosts with Mycobacterium bovis and the diagnostic difficulties of the ‘no visible lesion’ presentation , 2009, New Zealand veterinary journal.

[21]  Mahavir Singh,et al.  Immunological responses and protective immunity in BCG vaccinated badgers following endobronchial infection with Mycobacterium bovis. , 2009, Vaccine.

[22]  L. Peña,et al.  Disseminated Bovine Tuberculosis in a Wild Red Fox (Vulpes vulpes) in Southern Spain , 2008, Journal of wildlife diseases.

[23]  Mahavir Singh,et al.  Antigen specific immunological responses of badgers (Meles meles) experimentally infected with Mycobacterium bovis. , 2008, Veterinary immunology and immunopathology.

[24]  R. G. Hewinson,et al.  Validation of the BrockTB Stat-Pak Assay for Detection of Tuberculosis in Eurasian Badgers (Meles meles) and Influence of Disease Severity on Diagnostic Accuracy , 2008, Journal of Clinical Microbiology.

[25]  C. Gortázar,et al.  Evidence of the role of European wild boar as a reservoir of Mycobacterium tuberculosis complex. , 2008, Veterinary microbiology.

[26]  Eithne Costello,et al.  Experimental tuberculosis in the European badger (Meles meles) after endobronchial inoculation of Mycobacterium bovis: I. Pathology and bacteriology. , 2007, Research in veterinary science.

[27]  N. Walker,et al.  Bovine tuberculosis infection in wild mammals in the South-West region of England: a survey of prevalence and a semi-quantitative assessment of the relative risks to cattle. , 2007, Veterinary journal.

[28]  P. Caley,et al.  Surveillance of wildlife for Mycobacterium bovis infection using culture of pooled tissue samples from ferrets (Mustela furo) , 2005, New Zealand veterinary journal.

[29]  L. H. Taylor,et al.  Identifying Reservoirs of Infection: A Conceptual and Practical Challenge , 2002, Emerging infectious diseases.

[30]  J. Griffin,et al.  Transmission of Mycobacterium bovis from experimentally infected ferrets to non-infected ferrets (Mustela furo) , 2000, New Zealand veterinary journal.

[31]  J. Griffin,et al.  Partial protection against oral challenge with Mycobacterium bovis in ferrets (Mustela furo) following oral vaccination with BCG. , 1999, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

[32]  R. Barrett,et al.  A survey of mycobacteriosis of feral pigs in the Northern Territory. , 1981, Australian veterinary journal.

[33]  G. Hewinson,et al.  Advanced granulomatous lesions in Mycobacterium bovis-infected cattle are associated with increased expression of type I procollagen, gammadelta (WC1+) T cells and CD 68+ cells. , 2005, Journal of comparative pathology.